A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616026



Internal ID20989097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74299809..74310822hg38UCSC Ensembl
chr7:73714139..73725152hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3811014
hg1911014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226270
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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